4-(5-Methyl-1,3,4-oxadiazol-2-yl)piperidine

Base Information

• Chemical Name: 4-(5-Methyl-1,3,4-oxadiazol-2-yl)piperidine
• CAS No.: 161609-79-6
• Molecular Formula: C8H13 N3 O
• Molecular Weight: 167.211
• Hs Code.: 2934999090
• European Community (EC) Number: 824-959-7
• ChEMBL ID: CHEMBL1187446
• DSSTox Substance ID: DTXSID60597542
• Wikidata: Q82493120
• Mol file: 161609-79-6.mol

Synonyms:161609-79-6;4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine;2-METHYL-5-(PIPERIDIN-4-YL)-1,3,4-OXADIAZOLE;2-methyl-5-piperidin-4-yl-1,3,4-oxadiazole;Piperidine, 4-(5-methyl-1,3,4-oxadiazol-2-yl)-;CHEMBL502932;MFCD16294677;F2184-0013;SCHEMBL978682;CHEMBL1187446;DTXSID60597542;NEHQWJALQCSBBX-UHFFFAOYSA-N;AMY24053;BDBM50273110;MFCD09750319;AKOS005174711;KS-7844;DB-012912;VU0494857-1;EN300-146605;W18262;2-methyl-5-(4-piperidinyl)-1,3,4-oxadiazole;4-(5-Methyl-[1,3,4]oxadiazol-2-yl)-piperidine;A810278;Z1198222742;4-(5-Methyl-[1,3,4]oxadiazol-2-yl)-piperidine Hydrochloride

Chemical Property of 4-(5-Methyl-1,3,4-oxadiazol-2-yl)piperidine

Chemical Property:

• Vapor Pressure: 0.00143mmHg at 25°C
• Boiling Point: 296.5oC at 760 mmHg
• Flash Point: 133.1oC
• PSA: 50.95000
• Density: 1.098g/cm3
• LogP: 1.17380
• XLogP3: 0.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 167.105862047
• Heavy Atom Count: 12
• Complexity: 147

Purity/Quality:

97% ^*data from raw suppliers

4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=NN=C(O1)C2CCNCC2

Technology Process of 4-(5-Methyl-1,3,4-oxadiazol-2-yl)piperidine

There total 1 articles about 4-(5-Methyl-1,3,4-oxadiazol-2-yl)piperidine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ piperidine (110-89-4) + 4-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidine hydrobromide (161609-79-6)

Guidance literature:

Reference yield:

4-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidine hydrobromide (161609-79-6) + 4-chloro-2-((5-methyl-2H-tetrazol-2-yl)methyl)benzyl 1H-imidazole-1-carboxylate → 4-chloro-2-((5-methyl-2H-tetrazol-2-yl)methyl)benzyl 4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine-1-carboxylate

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 60 ℃; for 18h;

Reference yield:

4-(5-methyl-[1,3,4]oxadiazol-2-yl)-piperidine hydrobromide (161609-79-6) + (E)-3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethoxy)phenyl)acrylic acid → (E)-1-(4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidin-1-yl)-3-(2-((5-methyl-2H-tetrazol-2-yl)methyl)-4-(trifluoromethoxy)phenyl)prop-2-en-1-one

Guidance literature:

With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; In dichloromethane; ethyl acetate; at 20 ℃; for 2h;

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